A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576078



Internal ID16363487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77270084..77275705hg38UCSC Ensembl
Innerchr17:75266166..75271787hg19UCSC Ensembl
Innerchr17:72777761..72783382hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg385622
hg195622
hg185622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5786n54
Supporting Variantsnssv876231
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576078
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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